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Prasugrel

NDC 65162-001, Prasugrel, tablet, film coated, from Amneal Pharmaceuticals LLC.

Product NDC
65162-001
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205913
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRASUGREL HYDROCHLORIDE5 mg/1

Pharmacologic classes

Decreased Platelet Aggregation [PE]; P2Y12 Platelet Inhibitor [EPC]; P2Y12 Receptor Antagonists [MoA]

Package NDCNDC-11Package
65162-001-036516200010330 TABLET, FILM COATED in 1 BOTTLE (65162-001-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/406cc201-89b6-43cc-9e14-a59327a5b4d8

Use it

Look up 65162-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-001. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.